US4962095AExpiredUtility

Method of reducing pre-and post-ischemic myocardial arrhythmias and fibrillation

68
Assignee: SQUIBB & SONS INCPriority: Feb 15, 1989Filed: Dec 18, 1989Granted: Oct 9, 1990
Est. expiryFeb 15, 2009(expired)· nominal 20-yr term from priority
A61K 38/49A61K 31/40A61K 38/166A61K 31/675
68
PatentIndex Score
33
Cited by
17
References
5
Claims

Abstract

Zofenopril, fosinopril, (S)-1-[6-amino-2-[[hydroxy (4-phenylbutyl) phosphinyl]oxy]-1-oxohexyl]-L-proline or a pharmaceutically acceptable salt thereof alone or in combination with a thrombolytic, antiarrhythmic, or antifibrillatory agent is employed to reduce pre-and post- ischemic myocardial arrhythmias and fibrillations as well as reducing arrhythmias associated with congestive heart failure.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A method of reducing pre- and post-ischemic arrhythmias and fibrillation as well as reducing arrhythmias associated with congestive heart failure in a mammalian species which comprises administering to a mammalian species in need of such treatment an effective amount of (S)-1-[6-amino-2-[[hydroxy(4-phenylbutyl)phosphinyl]oxy]-1-oxohexyl]-L-proline or a pharmaceutically acceptable salt thereof alone or in combination with a thrombolytic agent, antiarrhythmic agent, or antifibrillatory agent or with a non-pharmaceutical reperfusion technique. 
     
     
       2. The method of claim 1 wherein the only therapeutic agent employed is (S)-1-[6-amino-2-[[hydroxy(4-phenylbutyl)phosphinyl]oxy]-1-oxohexyl]-L-proline or a pharmaceutically acceptable salt thereof. 
     
     
       3. The method of claim 1 wherein the agents employed are (S)-1-[6-amino-2-[[hydroxy(4-phenylbutyl)phosphinyl]oxy]-1-oxohexyl]-L-proline or a pharmaceutically acceptable salt thereof and a thrombolytic agent, an antiarrhythmia agent, or an antifibrillatory agent. 
     
     
       4. The method of claim 3 wherein the other agent is a thrombolytic agent selected from the group consisting of tissue plasminogen activator (tPA), recombinant tissue plasminogen activator, streptokinase, urokinase, and prourokinase. 
     
     
       5. The method of claim 3 wherein the other agent is an antiarrhythmic or antifibrillatory agent selected from the group consisting of quinidine, procainamide, disopyramide, lidocaine, tocainide, phenyltoin, flecainide, encainide, amiodarone, bretylium, clofilium, verapamil, diltiazem, propanolol, sotalol, nadolol, and metoprolol.

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